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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050987Generated: October 25, 2026

Water → 2-tert-Butyl-6-chloro-7-(4-methylpiperazine-1-sulfonyl)-benzooxazole

https://huagongshe.com/reaction/1050987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant1-MethylpiperazineHCID 53167—
Reactant2-Tert-butyl-6-chlorobenzoxazole-7-sulfonyl chlorideHCID 23447791—
SolventTetrahydrofuranHCID 8028—
Product2-tert-Butyl-6-chloro-7-(4-methylpiperazine-1-sulfonyl)-benzooxazoleHCID 2344783698.7%

Reaction Steps

1.62 ml (11.68 mmol; 1.2 eq) of triethylamine followed by 1.20 ml (10.71 mmol; 1.1 eq) of 1-methylpiperazine were added to a solution of 3.0 g (9.73 mmol; 1.0 eq) of 2-tert-butyl-6-chlorobenzoxazole-7-sulfonyl chloride (commercial ?) in 45 ml of tetrahydrofuran. The reaction medium was stirred at ambient temperature for 2 hours. Water was added and the reaction medium was extracted with ethyl acetate. The organic phases were combined, dried over magnesium sulfate, filtered and evaporated. 3.57 g of 2-tert-butyl-6-chloro-7-(4-methylpiperazine-1-sulfonyl)benzooxazole were obtained in the form of a tacky brown foam. Yield=98%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388149B2
Source datasetuspto-grants-2016_07
ORD IDord-9362f4fff4804733a378377229d494bf
Source noteuspto-grants-2016_07